Australia TGA ARTG recordLens, intraocular, posterior chamber
Australia TGA ARTG Registered Device · IQ Medical · Caregroup Sight Solution Private Ltd · Class IIb · Started May 10, 2024
Good Name: IQ Medical - Lens, intraocular, posterior chamber
- Risk Class
- Class IIb
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- May 10, 2024
- Effective Date
- May 10, 2024
- Name
- IQ Medical
- Country
- India
- Address
- Block No 310/C&E Village Dabhasa Taluka - Padra, Dist Vadodara, Gujarat, 391440
A device made of acrylic material intended to be implanted permanently in the posterior chamber of the eye, to replace the natural cataractous crystalline human eye lens. This implanted posterior chamber intraocular lens is intended to restore useful vision and is implanted following cataract removal.
Access comprehensive regulatory information for Lens, intraocular, posterior chamber in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is sponsored by IQ Medical, manufactured by Caregroup Sight Solution Private Ltd in India. The device registration started on May 10, 2024.
This page provides complete registration details including sponsor information, manufacturer details, and regulatory compliance data from the official Australia TGA ARTG medical device database. Pure Global AI offers free access to Australia's complete medical device registry with 131,000+ devices, helping global MedTech companies navigate TGA regulations efficiently.